Increased neutrophil extracellular trap formation promotes thrombosis in myeloproliferative neoplasms

Neutrophil Extracellular Traps Kill Bacteria

Brinkmann, V., Reichard, U., Goosmann, C., Fauler, B., Uhlemann, Y., Weiss, D. S., Weinrauch, Y., & Zychlinsky, A. (2004) · Science · doi:10.1126/science.1092385 · Cited by 10,268

Age-related clonal hematopoiesis associated with adverse outcomes

Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841

Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence

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Extracellular DNA traps promote thrombosis

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A double-blind, placebo-controlled trial of ruxolitinib for myelofibrosis

Verstovsek, S., Mesa, R. A., Gotlib, J., Levy, R. S., Gupta, V., DiPersio, J. F., Catalano, J. V., Deininger, M., Miller, C., Silver, R. T., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1110557 · Cited by 2,103

Somatic Mutations of Calreticulin in Myeloproliferative Neoplasms

Klampfl, T., Gisslinger, H., Harutyunyan, A. S., Nivarthi, H., Rumi, E., Milosevic, J. D., Them, N. C. C., Berg, T., Gisslinger, B., Pietra, D., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1311347 · Cited by 2,003

Histone hypercitrullination mediates chromatin decondensation and neutrophil extracellular trap formation

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PAD4 is essential for antibacterial innate immunity mediated by neutrophil extracellular traps

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Diabetes primes neutrophils to undergo NETosis, which impairs wound healing

Wong, S. L., Demers, M., Martinod, K., Gallant, M., Wang, Y., Goldfine, A. B., Kahn, C. R., & Wagner, D. D. (2015) · Nature Medicine · doi:10.1038/nm.3887 · Cited by 1,264

Neutrophil extracellular traps promote deep vein thrombosis in mice

Brill, A. G., Fuchs, T. A., Savchenko, A. S., Thomas, G. M., Martinod, K., Meyer, S. F. D., Bhandari, A. A., & Wagner, D. D. (2011) · Journal of Thrombosis and Haemostasis · doi:10.1111/j.1538-7836.2011.04544.x · Cited by 933

Increased levels of NETosis in myeloproliferative neoplasms are not linked to thrombotic events

Schmidt, S. U., Daniliants, D., Hiller, E., Gunsilius, E., Wolf, D. G. F., & Feistritzer, C. (2021) · Blood Advances · doi:10.1182/bloodadvances.2020004061 · Cited by 21

Prognostic Significance of NLR About NETosis and Lymphocytes Perturbations in Localized Renal Cell Carcinoma With Tumor Thrombus

Shang, B., Guo, L., Shen, R., Cao, C., Xie, R., Jiang, W., Wen, L., Bi, X., Shi, H., Zheng, S., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.771545 · Cited by 21

Somatic Mosaicism in Biology and Disease

Ogawa, H., Horitani, K., Izumiya, Y., & Sano, S. (2021) · Annual Review of Physiology · doi:10.1146/annurev-physiol-061121-040048 · Cited by 22

Thrombotic and Hemorrhagic Issues Associated with Myeloproliferative Neoplasms

Papageorgiou, L., Elalamy, I., Dreden, P. V., & Gerotziafas, G. (2022) · Clinical and Applied Thrombosis/Hemostasis · doi:10.1177/10760296221097969 · Cited by 20

Interferon alpha‐2 treatment reduces circulating neutrophil extracellular trap levels in myeloproliferative neoplasms

Massarenti, L., Knudsen, T. A., Enevold, C., Skov, V., Kjær, L., Larsen, M. K., Larsen, T. S., Hansen, D. L., Hasselbalch, H. C., & Nielsen, C. H. (2023) · British Journal of Haematology · doi:10.1111/bjh.18845 · Cited by 20

Citrullination and the protein code: crosstalk between post-translational modifications in cancer

Harada, K., Carr, S. M., Shrestha, A., & Thangue, N. B. L. (2023) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2022.0243 · Cited by 20

Prevention and Management of Thrombosis in BCR/ABL-Negative Myeloproliferative Neoplasms

Falanga, A., Marchetti, M., & Schieppati, F. (2021) · Hämostaseologie · doi:10.1055/a-1334-3259 · Cited by 20

Neutrophil Death in Myeloproliferative Neoplasms: Shedding More Light on Neutrophils as a Pathogenic Link to Chronic Inflammation

Marković, D. C., Maslovarić, I. S., Djikić, D., & Čokić, V. P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031490 · Cited by 20

Neutrophil swarming: Is a good offense the best defense?

Brown, L., & Yipp, B. G. (2023) · iScience · doi:10.1016/j.isci.2023.107655 · Cited by 19

Neutrophil extracellular traps (NETs) and fibrotic diseases

Wu, X., & Yang, Y. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.112085 · Cited by 19

IRGM/Irgm1 deficiency inhibits neutrophil-platelet interactions and thrombosis in experimental atherosclerosis and arterial injury

Sun, S. Y., Zou, X., Wang, D., Liu, Y., Zhang, Z., Guo, J., Lu, R., Huang, W., Wang, S., Li, Z., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.114152 · Cited by 18

Tissue mosaicism following stem cell aging: blood as an exemplar

Kapadia, C. D., & Goodell, M. A. (2024) · Nature Aging · doi:10.1038/s43587-024-00589-0 · Cited by 18

Neutrophil and Eosinophil Extracellular Traps in Hodgkin Lymphoma

Francischetti, I. M. B., Alejo, J. C., Sivanandham, R., DAVIES-HILL, T. M., Fetsch, P. A., Pandrea, I., Jaffe, E. S., & Pittaluga, S. (2021) · HemaSphere · doi:10.1097/hs9.0000000000000633 · Cited by 18

Interferon-alpha2 treatment of patients with polycythemia vera and related neoplasms favorably impacts deregulation of oxidative stress genes and antioxidative defense mechanisms

Skov, V., Thomassen, M., Kjær, L., Ellervik, C., Larsen, M. K., Knudsen, T. A., Kruse, T. A., & Hasselbalch, H. C. (2022) · PLoS ONE · doi:10.1371/journal.pone.0270669 · Cited by 18

Clinical Significance of Clonal Hematopoiesis of Indeterminate Potential in Hematology and Cardiovascular Disease

Hoermann, G. (2022) · Diagnostics · doi:10.3390/diagnostics12071613 · Cited by 17

Platelets from patients with myeloproliferative neoplasms have increased numbers of mitochondria that are hypersensitive to depolarization by thrombin

Ross, D. M., Liang, H., Iqra, Z., Whittaker, S. P., Tan, C. W., Dale, B. J., & Chen, V. M. Y. (2023) · Scientific Reports · doi:10.1038/s41598-023-36266-2 · Cited by 17

ROP-ET: a prospective phase III trial investigating the efficacy and safety of ropeginterferon alfa-2b in essential thrombocythemia patients with limited treatment options

Kiladjian, J., Ferrer‐Marín, F., Al‐Ali, H. K., Álvarez‐Larrán, A., Beggiato, E., Bieniaszewska, M., Breccia, M., Buxhofer‐Ausch, V., Černá, O., Crişan, A. M., et al. (2024) · Annals of Hematology · doi:10.1007/s00277-024-05665-4 · Cited by 17

Bioinformatics Analysis of Key Genes and Pathways Associated with Thrombosis in Essential Thrombocythemia

Guo, C., & Li, Z. (2019) · Medical Science Monitor · doi:10.12659/msm.918719 · Cited by 17

Clonal hematopoiesis of indeterminate potential and cardiovascular disease

Saadatagah, S., & Ballantyne, C. M. (2022) · Translational research · doi:10.1016/j.trsl.2022.08.013 · Cited by 17

Worsening Thrombotic Complication of Atherosclerotic Plaques Due to Neutrophils Extracellular Traps: A Systematic Review

Nappi, F., Bellomo, F., & Singh, S. S. A. (2023) · Biomedicines · doi:10.3390/biomedicines11010113 · Cited by 17

Somatic GATA2 mutations define a subgroup of myeloid malignancy patients at high risk for invasive fungal disease

Vedula, R. S., Cheng, M. P., Ronayne, C. E., Farmakiotis, D., Ho, V. T., Koo, S., Marty, F. M., Lindsley, R. C., & Bold, T. D. (2020) · Blood Advances · doi:10.1182/bloodadvances.2020002854 · Cited by 17

Extracellular neutrophil traps (NETs) in the pathogenesis of thrombosis and thromboinflammation

Bitsadze, V. O., Викторовна, С. Е., Khizroeva, J. K., Tretyakova, M. V., Shkoda, A. S., Radetskaya, L. S., Makatsariya, A. D., Elalamy, I., Gris, J., & Grandone, E. (2021) · Annals of the Russian academy of medical sciences · doi:10.15690/vramn1395 · Cited by 17

CXCL8 and its cognate receptors CXCR1/CXCR2 in primary myelofibrosis

Vermeersch, G., Proost, P., Struyf, S., Gouwy, M., & Devos, T. (2024) · Haematologica · doi:10.3324/haematol.2023.284921 · Cited by 16

Advances in Molecular Understanding of Polycythemia Vera, Essential Thrombocythemia, and Primary Myelofibrosis: Towards Precision Medicine

Tashkandi, H., & Younes, I. E. (2024) · Cancers · doi:10.3390/cancers16091679 · Cited by 16

How I Manage Thrombotic/Thromboembolic Complications in Myeloproliferative Neoplasms

Koschmieder, S. (2020) · Hämostaseologie · doi:10.1055/s-0040-1701474 · Cited by 16

Neutrophil Extracellular Traps in Cardiovascular Diseases: Pathological Roles and Therapeutic Implications

Ma, Y., Zhang, J., Qi, Y., Lu, Y., Dong, Y., & Hu, D. (2025) · Biomolecules · doi:10.3390/biom15091263 · Cited by 15

The role of NETosis in the pathogenesis of immunoinflammatory rheumatic diseases

Nasonov, E. L., Avdeeva, A. S., Reshetnyak, T. M., Aleksankin, A. P., & Rubtsov, Y. P. (2023) · Rheumatology Science and Practice · doi:10.47360/1995-4484-2023-513-530 · Cited by 15

New advances in the role of JAK2 V617F mutation in myeloproliferative neoplasms

Zhang, Y., Zhao, Y., Liu, Y., Zhang, M., & Zhang, J. (2024) · Cancer · doi:10.1002/cncr.35559 · Cited by 15

Pathological roles of NETs-platelet synergy in thrombotic diseases: From molecular mechanisms to therapeutic targeting

Li, J., Geng, Y., Luo, Y., Sun, X., Guo, Y., & Dong, Z. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114934 · Cited by 16

Neutrophil-to-Lymphocyte ratio as surrogate for JAK2V617F suppression and event-free survival in polycythemia vera

Barbui, T., Ghirardi, A., Empson, V. G., Fenili, F., Loscocco, G. G., Condorelli, A., Iurlo, A., Cattaneo, D., Rossi, E., Stefano, V. D., et al. (2025) · Blood Cancer Journal · doi:10.1038/s41408-025-01317-6 · Cited by 15

Clonal hematopoiesis and cardiovascular disease in cancer patients and survivors

Fuster, J. J. (2022) · Thrombosis Research · doi:10.1016/j.thromres.2021.12.009 · Cited by 15

Experimental Modeling of Myeloproliferative Neoplasms

Lanikova, L., Babošová, O., & Prchal, J. T. (2019) · Genes · doi:10.3390/genes10100813 · Cited by 15

JAK2 (and other genes) be nimble with MPN diagnosis, prognosis, and therapy

Ciboddo, M., & Mullally, A. (2018) · Hematology · doi:10.1182/asheducation-2018.1.110 · Cited by 15

Revisiting Circulating Extracellular Matrix Fragments as Disease Markers in Myelofibrosis and Related Neoplasms

Hasselbalch, H. C., Junker, P., Skov, V., Kjær, L., Knudsen, T. A., Larsen, M. K., Holmström, M. O., Andersen, M. H., Jensen, C., Karsdal, M. A., et al. (2023) · Cancers · doi:10.3390/cancers15174323 · Cited by 14

Clonal hematopoiesis of indeterminate potential (CHIP) in cerebromicrovascular aging: implications for vascular contributions to cognitive impairment and dementia (VCID)

Kállai, A., Ungvari, A., Csabán, D., Őrfi, Z., Lehoczki, A., Harasztdombi, J., Yabluchanskiy, A., Benyó, Z., Szappanos, Á., Tarantini, S., et al. (2025) · GeroScience · doi:10.1007/s11357-025-01654-1 · Cited by 14

Management of Patients with Acute Coronary Syndrome and Cancer

Moran, T. B., & Plana, J. C. (2020) · Current Cardiology Reports · doi:10.1007/s11886-020-01409-8 · Cited by 14

Resident Self-Tissue of Proinflammatory Cytokines Rather Than Their Systemic Levels Correlates with Development of Myelofibrosis in Gata1low Mice

Zingariello, M., Verachi, P., Gobbo, F., Martelli, F., Falchi, M., Mazzarini, M., Valeri, M., Sarli, G., Marinaccio, C., Melo‐Cardenas, J., et al. (2022) · Biomolecules · doi:10.3390/biom12020234 · Cited by 14

Casting a NET on cancer: the multiple roles for neutrophil extracellular traps in cancer

Wolach, O., & Martinod, K. (2021) · Current Opinion in Hematology · doi:10.1097/moh.0000000000000690 · Cited by 14

Therapy-Related Clonal Hematopoiesis

Yura, Y., Cochran, J. D., & Walsh, K. X. (2022) · Heart Failure Clinics · doi:10.1016/j.hfc.2022.02.010 · Cited by 14

Refractory livedoid vasculopathy in a child successfully treated with baricitinib

Zhang, H., Chen, J., Wu, N., Chen, H., & Liu, Y. (2022) · Dermatologic Therapy · doi:10.1111/dth.15659 · Cited by 14

Targeting neutrophil extracellular traps: A novel strategy in hematologic malignancies

Liu, R., Zhang, J., Rodrigues‐Lima, F., Zeng, J., & Nian, Q. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116334 · Cited by 14

Jak -ing Up the Plaque’s Lipid Core…and Even More

Libby, P., Molinaro, R., Sellar, R. S., & Ebert, B. L. (2018) · Circulation Research · doi:10.1161/circresaha.118.314074 · Cited by 14

Exacerbation of thromboinflammation by JAK2 V617F mutation worsens the prognosis of cerebral venous sinus thrombosis

Bourrienne, M., Duchez, V. L. C., Faille, D., Farkh, C., Nomenjanahary, M. S., Gay, J., Loyau, S., Journé, C., Dupont, S., Ollivier, V., et al. (2024) · Blood Advances · doi:10.1182/bloodadvances.2023011692 · Cited by 13

Social, Behavioral, and Clinical Risk Factors Are Associated with Clonal Hematopoiesis

Young, C. D., Hubbard, A. K., Saint‐Maurice, P. F., Chan, I. C. C., Cao, Y., Tran, D., Bolton, K. L., Chanock, S. J., Matthews, C. E., Moore, S. C., et al. (2024) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-24-0620 · Cited by 13

Clonal Hematopoiesis in Cancer and Cardiovascular Disease

Evans, M. A., & Walsh, K. X. (2025) · JACC CardioOncology · doi:10.1016/j.jaccao.2025.06.006 · Cited by 14

Lessons from mouse models of MPN

Benlabiod, C., Dagher, T., Marty, C., & Villeval, J. (2021) · International review of cytology · doi:10.1016/bs.ircmb.2021.02.009 · Cited by 13

The Role of Neutrophilic Granulocytes in Philadelphia Chromosome Negative Myeloproliferative Neoplasms

Kiem, D., Wagner, S. M., Magnes, T., Egle, A., Greil, R., & Melchardt, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22179555 · Cited by 13

Evaluation of Therapeutic Strategies to Reduce the Number of Thrombotic Events in Patients With Polycythemia Vera and Essential Thrombocythemia

Tremblay, D. A., Kosiorek, H., Dueck, A. C., & Hoffman, R. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.636675 · Cited by 13

How I approach the treatment of thrombotic complications in patients with myeloproliferative neoplasms

Guy, A., Morange, P., & James, C. (2024) · Blood · doi:10.1182/blood.2024025627 · Cited by 12

Cardiovascular risk factors in myeloproliferative neoplasms: associations with survival and thrombotic outcomes

How, J., Leiva, O., Redd, R. A., Marneth, A. E., DeAngelo, D. J., Dieli-Conwright, C. M., El-Jawahri, A. R., Kamaz, B., Kim, C., Lindsley, R. C., et al. (2025) · Blood Vessels Thrombosis & Hemostasis · doi:10.1016/j.bvth.2025.100051 · Cited by 12

Clonal hematopoiesis of indeterminate potential and incidence of venous thromboembolism in older adults

Saadatagah, S., Kim, R. B., Sukumar, S., Uddin, M. M., Folsom, A. R., Cushman, M., Tang, W., Natarajan, P., Ballantyne, C. M., Lutsey, P. L., et al. (2025) · Journal of Thrombosis and Haemostasis · doi:10.1016/j.jtha.2025.03.042 · Cited by 12

A new insight: crosstalk between neutrophil extracellular traps and the gut-liver axis for nonalcoholic fatty liver disease

Yin, J., Zhu, Y., Liu, R., Wang, W., Wang, Z., & Wang, J. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1599956 · Cited by 12

Dual Nature of Neutrophil Extracellular Traps (NETs)—From Cancer’s Ally to Therapeutic Target

Buszka, K., Dompé, C., Derwich, K., Pieścikowska, I., Nowicki, M. O., & Budna, J. (2025) · Cells · doi:10.3390/cells14151200 · Cited by 12

NETs - as predictors and targets of supportive therapy for cancer treatment

Morawiec, M.-L., Kubina, R., Jabłońska, E., Ratajczak–Wrona, W., Stępień, S., Gołębski, M., & Mielczarek‐Palacz, A. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1666261 · Cited by 12

A feedback loop: Interactions between Inflammatory Signals and Clonal Hematopoiesis in Cardiovascular Disease

Li, J., Wang, C., Liu, J., Yu, Y., Liu, Y., Peng, Q., Liu, H., & Guan, X. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06370-5 · Cited by 12

The role of clonal haematopoiesis in cardiovascular diseases: epidemiology and experimental studies

Min, K. D., Kour, A., Sano, S., & Walsh, K. X. (2020) · Journal of Internal Medicine · doi:10.1111/joim.13130 · Cited by 12

Prevalence of definite antiphospholipid syndrome in carriers of the JAK2V617F mutation

Janjetovic, S., Beckmann, L., Holstein, K., Rolling, C. C., Thiele, B., Schafhausen, P., Schön, G., Bokemeyer, C., Länger, F. P., & Voigtlaender, M. (2020) · Thrombosis Research · doi:10.1016/j.thromres.2020.11.027 · Cited by 12

Putative Role of Neutrophil Extracellular Trap Formation in Chronic Myeloproliferative Neoplasms

Marković, D. C., Maslovarić, I. S., Kovačić, M. V., Vignjević, S., & Ilić, V. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054497 · Cited by 12

Molecular and clinical aspects relevant for counseling individuals with clonal hematopoiesis of indeterminate potential

Cacic, A. M., Schulz, F. I., Germing, U., Dietrich, S., & Gattermann, N. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1303785 · Cited by 12

The emerging importance and evolving understanding of clonal hematopoiesis in multiple myeloma

DeStefano, C. B., Gibson, S. J., Sperling, A. S., Richardson, P. G. G., Ghobrial, I. M., & Mo, C. C. (2022) · Seminars in Oncology · doi:10.1053/j.seminoncol.2022.01.009 · Cited by 11

Clinical and Therapeutic Implications of Clonal Hematopoiesis

Petrone, G. E. M., Turker, I., Natarajan, P., & Bolton, K. L. (2024) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-120722-100409 · Cited by 11

Genetics of age-related clonal hematopoiesis and atherosclerotic cardiovascular disease

Jung, C. H., Evans, M. A., & Walsh, K. X. (2020) · Current Opinion in Cardiology · doi:10.1097/hco.0000000000000726 · Cited by 11

Increased clonal hematopoiesis involving DNA damage response genes in patients undergoing lung transplantation

Tague, L. K., Oetjen, K. A., Mahadev, A., Walter, M. J., Anthony, H., Kreisel, D., Link, D. C., & Gelman, A. E. (2023) · JCI Insight · doi:10.1172/jci.insight.165609 · Cited by 11

Plaque erosion risk and JAK2 V617F variant

Wang, S., Luo, X., Hu, S., Zhao, C., Sun, Q., Zeng, M., Bao, X., Wang, Y., Wu, F., Yang, Y., et al. (2025) · European Heart Journal · doi:10.1093/eurheartj/ehaf114 · Cited by 10

Chronic Inflammation in Primary Myelofibrosis: In‐Depth Insights Into Pathogenesis and Promising Anti‐Inflammatory Therapeutic Strategies

Chen, M., Zheng, C., Zhang, Y., He, J., & Shi, Z. (2025) · Mediators of Inflammation · doi:10.1155/mi/9967975 · Cited by 10

Toward new therapy end points in polycythemia vera: targeting clonal and inflammatory pathways

Barbui, T., & Scandura, J. M. (2025) · Blood Advances · doi:10.1182/bloodadvances.2025018011 · Cited by 10

COVID-19 and myeloproliferative neoplasms: some considerations

Kamaz, B., & Mullally, A. (2020) · Leukemia · doi:10.1038/s41375-020-01070-8 · Cited by 10

Increased reactive oxygen species lead to overactivation of platelets in essential thrombocythemia

Dong, H., Li, H., Fang, L., Zhang, A., 刘晓帆, Xue, F., Chen, Y., Liu, W., Chi, Y., Wang, W., et al. (2023) · Thrombosis Research · doi:10.1016/j.thromres.2023.04.001 · Cited by 10

A neutrophil extracellular trap-related risk score predicts prognosis and characterizes the tumor microenvironment in multiple myeloma

Zhao, Z., Huo, Y., Du, Y., Huang, Y., Liu, H., Zhang, C.-T., & Yan, J. (2024) · Scientific Reports · doi:10.1038/s41598-024-52922-7 · Cited by 10

Clonal haematopoiesis of emerging significance

Hammond, D. E., & Loghavi, S. (2021) · Pathology · doi:10.1016/j.pathol.2021.02.005 · Cited by 10

Can Novel Insights into the Pathogenesis of Myeloproliferative Neoplasm-Related Thrombosis Inform Novel Treatment Approaches?

Wolach, O., & Abulafia, A. S. (2021) · Hemato · doi:10.3390/hemato2020018 · Cited by 10

Paraneoplastic Thromboembolism and Thrombophilia: Significance in Visceral Medicine

Pfrepper, C. (2020) · Visceral Medicine · doi:10.1159/000509150 · Cited by 10

Identification of Potential Key Genes and Regulatory Markers in Essential Thrombocythemia Through Integrated Bioinformatics Analysis and Clinical Validation

Wang, J., Wu, Y., Uddin, M. N., Chen, R., & Jian-ping, H. (2021) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s309166 · Cited by 10

The CHIP-clinic as the catalyst of preventive medicine

Hasselbalch, H. C., Skov, V., Kjær, L., Knudsen, T. A., Eickhardt‐Dalbøge, C. S., Ellervik, C., Cordua, S., Sørensen, A. L., Christensen, S. F., Kristiansen, M. H., et al. (2024) · Frontiers in Hematology · doi:10.3389/frhem.2024.1459154 · Cited by 9

Analytical Review: Neutrophil Extracellular Traps and Antiphospholipid syndrome

Butt, A., Sharda, A. V., Lee, A. I., & Knight, J. S. (2025) · Transfusion Medicine Reviews · doi:10.1016/j.tmrv.2025.150909 · Cited by 9

Inflammatory signaling in the pathogenesis of acute myeloid leukemia

Baumann, A., & Ellegast, J. M. (2025) · HemaSphere · doi:10.1002/hem3.70188 · Cited by 9

Cytokine Landscapes, Immune Dysregulation, and Treatment Perspectives in Philadelphia-Negative Myeloproliferative Neoplasms: A Narrative Review

Todor, S. B., & Mihăilă, R. G. (2025) · Journal of Clinical Medicine · doi:10.3390/jcm14176328 · Cited by 9

Pathogenesis of plaque erosion

Riascos‐Bernal, D. F., Quinones, G., Abdelaal, S. A., Menegus, M. A., & Sibinga, N. E. S. (2025) · Trends in Cardiovascular Medicine · doi:10.1016/j.tcm.2025.09.004 · Cited by 9

Neutrophil Extracellular Traps and Delayed Cerebral Ischemia in Patients With Subarachnoid Hemorrhage

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